2-(4-(1-Bromoethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
Reagent
Code: #46083
CAS Number
1422655-36-4
blur_circular Chemical Specifications
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Molecular Information
Weight
311.02 g/mol
Formula
C₁₄H₂₀BBrO₂
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Registry Numbers
MDL Number
MFCD24386346
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent. Its structure, featuring a boronate ester group, enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The bromoethyl group further enhances its reactivity, allowing for additional functionalization or substitution in targeted synthesis pathways. Its stability and compatibility with various reaction conditions make it a versatile tool in modern synthetic chemistry.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | solid |
| Purity | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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